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Clinical Trial Summary

The purpose of this study is to investigate how topical diclofenac use can improve functional mobility and physical activity primarily, as well as other quality-of-life (QoL) parameters such as sleep, mood, and engagement in daily activities in participants with knee OA.


Clinical Trial Description

This prospective open-label, single-arm, multi-country (United States [US] and European Union [EU]) real-world evidence study will be conducted in a hybrid form and will focus on assessing the impact of Voltaren Gel on functional mobility and QoL in individuals with mild/nonserious OA of the knee. Participants will be required to be physically present at the study site for screening, end of baseline and end of study visits. The remaining treatment will be conducted in a remote manner (for example, at home) to observe the real-world usage of Voltaren Gel. This study will utilize a research-grade validated wearable device: Actigraph, to accurately measure objective changes in functional mobility. Sufficient participants will be screened to enroll approximately 195 participants to ensure that around 147 of these participants will successfully complete the entire study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06379893
Study type Interventional
Source HALEON
Contact Haleon Response Center
Phone +441932959500
Email ww.clinical-trial-register@haleon.com
Status Recruiting
Phase Phase 4
Start date April 25, 2024
Completion date November 15, 2024

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